Why Therapeutic Trials Fail in Primary Tauopathies
Author:
Affiliation:
1. Parkinson and Other Movement Disorders Center, Department of Neurosciences University of California San Diego La Jolla California USA
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29322
Reference42 articles.
1. Evolving concepts in progressive supranuclear palsy and other 4-repeat tauopathies
2. Clinical Spectrum of Tauopathies
3. Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy
4. Validation of the Movement Disorder Society Criteria for the Diagnosis of 4‐Repeat Tauopathies
5. Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
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1. Antisense oligonucleotides provide optimism to the therapeutic landscape for tauopathies;Neural Regeneration Research;2024-05-13
2. Genetic forms of tauopathies: inherited causes and implications of Alzheimer’s disease-like TAU pathology in primary and secondary tauopathies;Journal of Neurology;2024-03-30
3. Total Patient Delay: A Comparison of Patient and Clinician/Health System Delays in the Diagnosis of Progressive Supranuclear Palsy and Corticobasal Syndrome;Movement Disorders Clinical Practice;2024-02-18
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